Investigational drugs for the treatment of spinal cord injury: review of preclinical studies and evaluation of clinical trials from Phase I to II

被引:26
作者
Nagoshi, Narihito [1 ,2 ]
Fehlings, Michael G. [1 ,3 ]
机构
[1] Univ Hlth Network, Toronto Western Hosp, Krembil Neurosci Ctr, Toronto, ON M5T 2S8, Canada
[2] Keio Univ, Sch Med, Dept Orthopaed Surg, Tokyo 1608582, Japan
[3] Univ Toronto, Univ Hlth Network, Inst Med Sci, Toronto, ON M5S 1A8, Canada
关键词
basic fibroblast growth factor; clinical trials in Phase II; magnesium; minocycline; Rho protein antagonist; riluzole; spinal cord injury; PROMOTES FUNCTIONAL RECOVERY; CHONDROITIN SULFATE PROTEOGLYCANS; CENTRAL-NERVOUS-SYSTEM; NEURITE OUTGROWTH; SECONDARY INJURY; WHITE-MATTER; NOGO-A; NEUROPROTECTIVE AGENT; CORTICOSPINAL TRACT; CEREBROSPINAL-FLUID;
D O I
10.1517/13543784.2015.1009629
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Efforts in basic research have clarified mechanisms involved in spinal cord injury (SCI), and resulted in positive findings using experimental treatments including cell transplantation and drug administration preclinically. Based on accumulated results, various clinical trials have begun for human SCI. Areas covered: In this review, the authors focus on five investigational drugs: riluzole, minocycline, Rho protein antagonist, magnesium chloride in polyethylene glycol formulation, and basic fibroblast growth factor. All drugs have established safety and tolerability from Phase I clinical trials, and are now in Phase II. They have been proven to have neuroprotective and/or neuroregenerative effects in animal models of SCI. Expert opinion: To date, diverse drugs have been translated into clinical trials, but none have reached clinical application. A key gap was the lack of reliable biomarkers for SCI to fast-track Phase I/II trials. Furthermore, problems were often due to lack of adequate outcome assessments for both animal models and SCI patients. In order to advance clinical trials more quickly and with greater success, more clinically relevant animal models should be used in basic research. Clinically, it is indispensable to use appropriate outcome measurements and to construct a wide network among clinical centers to validate the efficacy of drugs.
引用
收藏
页码:645 / 658
页数:14
相关论文
共 102 条
[1]   International Campaign for Cures of Spinal Cord Injury Paralysis (ICCP): another step forward for spinal cord injury research [J].
Adams, M ;
Cavanagh, JFR .
SPINAL CORD, 2004, 42 (05) :273-280
[2]  
Agrawal SK, 1996, J NEUROSCI, V16, P545
[3]  
[Anonymous], 2013, J SPINAL CORD MED, V36, P170
[4]   A SENSITIVE AND RELIABLE LOCOMOTOR RATING-SCALE FOR OPEN-FIELD TESTING IN RATS [J].
BASSO, DM ;
BEATTIE, MS ;
BRESNAHAN, JC .
JOURNAL OF NEUROTRAUMA, 1995, 12 (01) :1-21
[5]   A study of riluzole in the treatment of advanced stage or elderly patients with amyotrophic lateral sclerosis [J].
Bensimon, G ;
Lacomblez, L ;
Delumeau, JC ;
Bejuit, R ;
Truffinet, P ;
Meininger, V .
JOURNAL OF NEUROLOGY, 2002, 249 (05) :609-615
[6]   Chondroitinase ABC promotes functional recovery after spinal cord injury [J].
Bradbury, EJ ;
Moon, LDF ;
Popat, RJ ;
King, VR ;
Bennett, GS ;
Patel, PN ;
Fawcett, JW ;
McMahon, SB .
NATURE, 2002, 416 (6881) :636-640
[7]   RECOVERY FROM SPINAL-CORD INJURY MEDIATED BY ANTIBODIES TO NEURITE GROWTH-INHIBITORS [J].
BREGMAN, BS ;
KUNKELBAGDEN, E ;
SCHNELL, L ;
DAI, HN ;
GAO, D ;
SCHWAB, ME .
NATURE, 1995, 378 (6556) :498-501
[8]   Plasticity of the Injured Human Spinal Cord: Insights Revealed by Spinal Cord Functional MRI [J].
Cadotte, David W. ;
Bosma, Rachael ;
Mikulis, David ;
Nugaeva, Natalia ;
Smith, Karen ;
Pokrupa, Ronald ;
Islam, Omar ;
Stroman, Patrick W. ;
Fehlings, Michael G. .
PLOS ONE, 2012, 7 (09)
[9]   ANTIBODY AGAINST MYELIN-ASSOCIATED INHIBITOR OF NEURITE GROWTH NEUTRALIZES NONPERMISSIVE SUBSTRATE PROPERTIES OF CNS WHITE MATTER [J].
CARONI, P ;
SCHWAB, ME .
NEURON, 1988, 1 (01) :85-96
[10]   Results of a phase II placebo-controlled randomized trial of minocycline in acute spinal cord injury [J].
Casha, Steven ;
Zygun, David ;
McGowan, M. Dan ;
Bains, Ish ;
Yong, V. Wee ;
Hurlbert, R. John .
BRAIN, 2012, 135 :1224-1236